| Tag | Content |
|---|
EnhancerAtlas ID | HS130-13904 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr2:97151290-97152680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:97151952-97151970 | GGAAAGCGAAACTTAGCC | + | 6.61 | | SPIC | MA0687.1 | chr2:97152342-97152356 | GTCTTCCTCTTTTT | - | 6.22 | | Sox6 | MA0515.1 | chr2:97151896-97151906 | CCATTGTTTT | + | 6.02 | | Stat4 | MA0518.1 | chr2:97151946-97151960 | CTTCTAGGAAAGCG | + | 6.17 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65729 | chr2:97150674-97152957 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I096485 | chr2 | 97150742 | 97153281 |
|
Enhancer Sequence | AGAGGCACCA CCTCTAGATT CCTGTGGAGA TCCTACCACC CATTCCTTCA AAGGAAGGGA 60
CTGGGGAGCA GGGCAGCTGG CAGCAGAGGC TAATCTGCTG TGCAGGTCTG TGGAGGAAGG 120
GACCGTGCGC GGTTCTCTTC CCTCTGCCTC CAGGCTTAGG AGTCATCCCC CACACGCGGG 180
ACCCCCAGTC CCCACTGTAG ACTTCTTCCA AGTGGAATTT CTTCAACAGT TGATCAGCAG 240
GGGGGTCAGG GCGTGCAGTG CAGGGGTGGG GGTGGGGGTT GCGAGAGGAG TGCCATCAGG 300
GAGTAATGCT GGCGAGGCCT CATGAGGACA GCACGCTGGG GCCCTGTGTG CGATGGGCGC 360
CAGGGGCAGG TGACATGGTG GACCCGGTCT CCCCCTTCCC TCTCCAATTG ATCTAACAGA 420
AAGCCTGATG TGAAAGTCTG GACGAGGGAA TTTTCCCATA TCTGCAGGAA AGCCCCGTAG 480
CAGGTCCCTG GAGCCAGCCC GGGCAGGCCT CCGCTTACAG GACGCTAAAG ATCCCTGGTT 540
GCAGTTCTAC TTTCTTTTTA CTGCGTGTAT TCTGCCCCTG TGATAATGAT TCATTACACG 600
CTTCCTCCAT TGTTTTACTC CAGTGACCTC ACGTCAAGGG AACCTGTGAT CTCAGGCTTC 660
TAGGAAAGCG AAACTTAGCC GCAGCCTGCC TCTCTCCCAG CCTGCCTTAC AAGCACTGTG 720
AGTTGCTGGC TGGCCGAGGC CCTGGCAGAT CAGACCTCCT GCAGCCCCAG GGATGGCACG 780
GGCACCGCCA CTCACGCAGC CGGTAGAGCG CTCCTAGGGC AGGCCCATCT CGCTTCCCTC 840
TCGCCTCTCC CCCCCGCTTT TGCTTGGGCC AATCCGACCT CCTCACCTCC TCGTAGCTCC 900
CCCAGCACAC CTTGCCTTTG CCATCTCTGC ATGTGCCGCG CCTGCTGTCT GGAAGACCGG 960
CATCCATTCC CCTCTGCCTT CCAAACTCTC CCTGTAGGAC CAGCTCAAAA GGCATCTCCT 1020
CTTCAGCTGT TCCTGCTGCC AGGGCTAATA TCGTCTTCCT CTTTTTTCCC CACTAGCGCT 1080
TCTTTGTCTA TTTTGGAGAG GTTTTGTTTT GGATAACTTT TTAATTGAGA TGTAACTCAC 1140
ATTATCATAA TATTCGTCTT TTTTAAATGC ACAGTTCAAT GGTTTTTAGT ATTCTATTCA 1200
CAAAGTTGTG CAACTATCAG CATAATTAAT TTCAGGATAT TTTCCTCACC CTAAAAAGAA 1260
ACTCCGTACC CTTTAGTTGT CACTCCTCAT TTCTGCCTCT CCCCAGCCTC TGAAACCCAC 1320
TAATCTACTT TCTGTTTCTG GATTTGCCTA TTGTAGACAT TTCATATGGA TGGAATCGTG 1380
CATATATGGC 1390
|
